Introduction: One of the serious consequences of the SARS-CoV-2 pandemic is the shortage of protective equipment for health personnel. N95 masks are considered one of the essential protective equipment in the management of patients with COVID-19. The shortage of N95 masks implies potential health risks for health personnel and significant economic losses for the health institution. The objective of this work was to investigate the disinfection of N95 masks artificially contaminated with SARS-CoV-2 and ESKAPE bacteria by using hydrogen peroxide plasma. Material and methods: We examined the disinfection capacity of hydrogen peroxide plasma against the SARS-CoV-2 and 2 members of the ESKAPE bacteria (Acinetobacter baumannii and Staphylococcus aureus) through a study of artificial contamination in situ of N95 masks. Amplification of specific genes by real-time reverse transcription polymerase chain reaction of SARS-CoV-2 and microbiological culture of ESKAPE bacteria was performed before and after the disinfection process. Results: SARS-CoV-2 was not detected in all assays using 5 different concentrations of the virus, and A baumannii and S aureus were not cultivable with inoculums of 10 2 to 10 6 CFU after disinfection tests of N95 masks with hydrogen peroxide plasma. Conclusion: Disinfection of N95 masks by using the hydrogen peroxide plasma technology can be an alternative for their reuse in a shortage situation. Implications for the use of disinfection technologies of N95 masks and the safety of health personnel are discussed.
Extracellular vesicles (EVs) mediate many stages of tumor progression including angiogenesis, escape from immune surveillance, and extracellular matrix degradation. We studied whether EVs from plasma of women with breast cancer are able to induce an epithelial-mesenchymal transition (EMT) process in mammary epithelial cells MCF10A. Our findings demonstrate that EVs from plasma of breast cancer patients induce a downregulation of E-cadherin expression and an increase of vimentin and N-cadherin expression. Moreover, EVs induce migration and invasion, as well as an increase of NFκB-DNA binding activity and MMP-2 and MMP-9 secretions. In summary, our findings demonstrate, for the first time, that EVs from breast cancer patients induce an EMT-like process in human mammary non-tumorigenic epithelial cells MCF10A.
BackgroundFBN1 (15q21.1) encodes fibrillin-1, a large glycoprotein which is a major component of microfibrils that are widely distributed in structural elements of elastic and non-elastic tissues. FBN1 variants are responsible for the related connective tissue disorders, grouped under the generic term of type-1 fibrillinopathies, which include Marfan syndrome (MFS), MASS syndrome (Mitral valve prolapse, Aortic enlargement, Skin and Skeletal findings, Acromicric dysplasia, Familial ectopia lentis, Geleophysic dysplasia 2, Stiff skin syndrome, and dominant Weill-Marchesani syndrome.Case presentationTwo siblings presented with isolated skeletal manifestations of MFS, including severe pectus excavatum, elongated face, scoliosis in one case, and absence of other clinical features according to Ghent criteria diagnosis, were screened for detection of variants in whole FBN1 gene (65 exons). Both individuals were heterozygous for the R2726W variant. This variant has been previously reported in association with some skeletal features of Marfan syndrome in the absence of both tall stature and non-skeletal features. These features are consistent with the presentation of the siblings reported here.ConclusionThe presented cases confirm that the R2726W FBN1 variant is associated with skeletal features of MFS in the absence of cardiac or ocular findings. These findings confirm that FBN1 variants are associated with a broad phenotypic spectrum and the value of sequencing in atypical cases.
Background: The causative primary agent of urinary tract infections (UTI) is uropathogenic Escherichia coli (UPEC); however, commensal Escherichia coli (CEC) has been also implicated in the development of UTI. Due to the recent emergence of virulent and resistant strains, it is necessary to have evidence to demonstrate that UPEC and CEC are isolated from patients with UTI and subsequently they have the genes to be considered pathogenic. Objectives: To determine the distribution of resistance and virulence genes in UPEC and CEC strains isolated from the patients with UTI (hospitalized and ambulatory). Methods: One hundred seven E. coli strains were genotyped according to Clermont protocol and were subjected to PCR assays in order to detect resistance and virulence genes. In addition, the antimicrobial test in solid media was performed to determinate the correlation "pheno/genotype". Results: Genotyping analysis showed that group B2 (42.05%) was the most predominant, strains followed by A (27.1%), D (24.29%), and finally, B1 (6.54%). β-lactams, carbapenems, aminoglycosides, and nitrofurans showed the best activity. The virulence gene frequencies were: fimH (92/85.98%), iutA (68/63.55%), traT (66/61.68%), papC (36/33.64%), and cnf1 (15/14.02%) while resistance genes were: blaCTX-M(41/38.32%), blaOXA (49/45.79%), and blaSHV (2/1.87%). The associations fimH/blaCTX, fimH/blaOXA, traT/blaCTX, traT/blaOXA, iutA/blaCTX, and iutA/blaOXA showed higher incidence while the associations with cnf1 and papC genes were low. Conclusions: Uropathogenic E. coli has the necessary genetic elements (virulence and resistance) to be considered the main pathogen causing UTI in the Mexican population. Additionally, to our knowledge, there are no studies in our country demonstrating that the CEC isolated from the patients with UTI contains genetic elements of virulence and resistance that allow them to be potentially pathogenic.
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